eudamed_udi
Primary ID: 08049033198638
SERODRAIN (UDI 08049033198638)
Manufactured by Know Medical Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SERODRAIN - Primary ID 08049033198638
Device Regulatory Overview
The SERODRAIN (Model/Catalog Number: RAI1217) is a medical device manufactured by Know Medical Srl. This product is indexed under FDA Product Code / Category Classification A060202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RAI1217
- Product Code / EMDN
- A060202
- Device Name
- SERODRAIN - Ago Trocar 12CH
- Database Sync Date
- 2026-08-09 16:29:26
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SERODRAIN?
The registered manufacturer of record for SERODRAIN is Know Medical Srl.
What is the Primary UDI-DI identifier for SERODRAIN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08049033198638.
What classification code is assigned to this device?
This device is registered under product classification code A060202.
Similar Classification Devices (A060202)
Other Devices by Know Medical Srl
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